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1 olar range and high selectivity, relative to aldehyde reductase.
2 , and has high selectivity for aldose versus aldehyde reductase.
3 yme that we designate SCALD, for short-chain aldehyde reductase.
4 stitutive expression of both mouse and human aldehyde reductase.
5 onoamine oxidase, aldehyde dehydrogenase and aldehyde reductase.
6 carboxyl-containing substrate preference of aldehyde reductase.
7 e balance of O2 supply and removal of native aldehyde reductases.
8 , while being 5400 times less active against aldehyde reductase, a related enzyme involved in the det
9 f p-coumaraldehyde, likely the result of low aldehyde reductase activity (i.e. alcohol dehydrogenase
11 Pseudomonas putida (mdlC) and native E. coli aldehyde reductase (adhP) in E. coli BL21 star(DE3), the
12 rA- cells, suggesting that the Dictyostelium aldehyde reductase affects several metabolic pathways in
13 PGA1 elicited only marginal inhibition of aldehyde reductase (AKR1A1), considered responsible for
14 nstitutively and widely expressed human AKR, aldehyde reductase (AKR1A1), will oxidize potent proxima
16 nd Arg311, located in the C-terminal loop of aldehyde reductase, and not found in any other C-termina
17 se intermediaries, characteristic of hepatic aldehyde reductases, and to maintain osmoregulation, a f
18 ent in dog retinal capillary pericytes, with aldehyde reductase being the major reductase present.
19 ing mouse gene knock-out models, we identify aldehyde reductase (EC 1.1.1.2, Akr1a4 (GR)) and aldose
21 analyze the mechanism of basal regulation of aldehyde reductase expression, we cloned the murine gene
22 the regulation of its expression, the human aldehyde reductase gene and promoter were cloned and cha
24 In contrast to the mouse gene, the human aldehyde reductase gene has two alternatively spliced tr
30 hern blots of multiple tissues indicate that aldehyde reductase mRNA is present in all tissues examin
31 r with the broad-substrate specificity of an aldehyde reductase or an aldehyde decarbonylase, the cat
34 find that disrupting alrA, the gene encoding aldehyde reductase, results in the loss of alrA mRNA and
35 peaks corresponding to aldose reductase and aldehyde reductase, the latter being dominant, were obse
37 abidopsis gene (At1g10310) encoding a pterin aldehyde reductase was identified by searching the short
38 and comparison with the active site of human aldehyde reductase, whose structure is very similar.
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